Original source

Variants (including SNPs and indels) imported from dbSNP (release 144)|View in dbSNP

Alleles
G/A|Ancestral: G|Ambiguity code: R|MAF: 0.19 (A)
Location

Chromosome 16:20334293 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs386451413

HGVS names

This variant has 6 HGVS names - Show

Genotyping chips

This variant has assays on: Illumina_HumanOmni2.5, Affy GenomeWideSNP_6.0, Illumina_HumanOmni1-Quad

About this variant

This variant overlaps 5 transcripts and has 3761 sample genotypes.

Variant displays